Quinacrine hydrochlorideProduct ingredient for Quinacrine
- Name
- Quinacrine hydrochloride
- Drug Entry
- Quinacrine
An acridine derivative formerly widely used as an antimalarial but superseded by chloroquine in recent years. It has also been used as an anthelmintic and in the treatment of giardiasis and malignant effusions. It is used in cell biological experiments as an inhibitor of phospholipase A2.
- Accession Number
- DBSALT002386
- Structure
- Synonyms
- Mepacrine hydrochloride dihydrate / Quinacrine dihydrochloride dihydrate / Quinacrine HCl / Quinacrine hydrochloride dihydrate
- UNII
- G6242H2NAA
- CAS Number
- 6151-30-0
- Weight
- Average: 508.91
Monoisotopic: 507.1822251 - Chemical Formula
- C23H36Cl3N3O3
- InChI Key
- RZFNKJVCPDLQQA-UHFFFAOYSA-N
- InChI
- InChI=1S/C23H30ClN3O.2ClH.2H2O/c1-5-27(6-2)13-7-8-16(3)25-23-19-11-9-17(24)14-22(19)26-21-12-10-18(28-4)15-20(21)23;;;;/h9-12,14-16H,5-8,13H2,1-4H3,(H,25,26);2*1H;2*1H2
- IUPAC Name
- 6-chloro-N-[5-(diethylamino)pentan-2-yl]-2-methoxyacridin-9-amine dihydrate dihydrochloride
- SMILES
- O.O.Cl.Cl.CCN(CC)CCCC(C)NC1=C2C=C(OC)C=CC2=NC2=CC(Cl)=CC=C12
- External Links
- ChemSpider
- 2007115
- ChEMBL
- CHEMBL2105615
- Predicted Properties
Property Value Source Water Solubility 0.00239 mg/mL ALOGPS logP 6.13 ALOGPS logP 5.15 Chemaxon logS -5.2 ALOGPS pKa (Strongest Basic) 10.33 Chemaxon Physiological Charge 2 Chemaxon Hydrogen Acceptor Count 4 Chemaxon Hydrogen Donor Count 1 Chemaxon Polar Surface Area 37.39 Å2 Chemaxon Rotatable Bond Count 9 Chemaxon Refractivity 118.96 m3·mol-1 Chemaxon Polarizability 46.31 Å3 Chemaxon Number of Rings 3 Chemaxon Bioavailability 0 Chemaxon Rule of Five No Chemaxon Ghose Filter No Chemaxon Veber's Rule Yes Chemaxon MDDR-like Rule Yes Chemaxon